Variant #0000542078 (NC_000011.9:g.108143456C>G, NM_000051.3:c.3161C>G (ATM))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.108143456C>G |
| DNA change (hg38) |
g.108272729C>G |
| Published as |
ATM(NM_000051.3):c.3161C>G (p.P1054R, p.(Pro1054Arg), p.Pro1054Arg), ATM(NM_000051.4):c.3161C>G (p.P1054R) |
| ISCN |
- |
| DB-ID |
ATM_000490 See all 14 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.01657 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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